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Answer Questions 1-3 using compounds A-H below: ОН OH CI сн3 A C OH Но CHs...
please answer questions 1-4 Question 1 Which of the following is the most stable carbocation? СН3 V. CH2 What is the major product of the following reaction? Н HBO C CHS CH CH CH3-CH ( CH, Br CH2-CH-C–CH, Br Br CH CH CH3-CH:-¢-CH Br ін, CHE CH CH.-CH- Br CH. D Question 3 What is the major product of the following reaction? CH, НО 1 Оснок IV. CH2OH CH3 "О" ОН Д. он СН3 CH3 Но Ш. CH, ОН Question...
Qualitative Analysis of Organic Compounds: Pre lab questions (5 pts) 1. (1 point) Identify the functional groups based on color / odor a. Dark yellow to red color indicates that the functional group could possibly be------------- b. Fruity / Floral odor indicates that the functional group could possibly be------------- c. Fishy odor indicates that the functional group could possibly be------------- d. Sharp, biting odor indicates that the functional group could possibly be------------- 2. (0.5 pts) If a liquid is soluble...
4. Answer the following questions regarding the compounds given below: CH,OH HOM н -он сон CI (11) (iv) Hm. a) Give a systematic name for compounds III and IV (6 points) b) Draw a newman projection of a staggered conformation for compound III, viewed down the C2- bond. (2 points)
Which of the following chiral compounds is(are) R enantiomer(s)? 1) I. II III но, CI. Н,с CH CI OH н,с 2) You found an organic compound containing chiral carbon atom with the following four substituents: HC C-, CI-, O C- and H2C-CH-, What would be the correct order of their priorities? A) HC C-> O-C->CI-> H2C-CH B) Cl->HCC-> 0-C-> H2C-CH C) Cl-> O C-> HC C-> H2C-CH D) Cl-> O-C-> H2C-CH-> HC C E) O-C-> Cl-> HC C-> H2C-CH 3)...
2) CHs LDA 1) LDA 3 2) Ci OH, H20 -OH, H2O CHO 1 LDA 2) CH3CH2Br Он, H2O 1) NaOEt 8 2) NaOEt OEt 10 Cl NaH 2 (excess) 12 HO Bra(excess) 13 HO LDA 14L THF, -78 C NaOEt, EtOH NaOEt, EtOH 16 NaOEt, EtOH 17 Br но 18 OOEt 1)NaOEt, EtOH 2) H3O 19 OEt 20 l HO o CHO + H20
IDENTIFICATION of an UNKNOWN ORGANIC COMPOUND PRE LAB QUESTIONS DATE NAME 1. Circle AND name four different functional groups in the compound to the right Macrocyclic lactone ring н сн N сн но. Нас Cн, O HO -O -он CH3 Hyc-OH CH3 Cн HyC OCH OH CH CH3 "сна 2. You have an unknown containing five carbon atoms, has a pH of 6, yields a yellow solution having no precipitate in a 2,4-DNP test, and produces a Jell-O like blue-green...
н'-н,о) HS Raney Ni HS H'-но) + Н Но CH2OH NH2 CI 1) LAH ОН 2) H,О ZI Question 1 (6 points). Provide IUPAC names for the following structures. Question 2 (14 points). Convert the following IUPAC names into structures. 2,4-dimethylcyclopent-2-enone 5-hydroxy-2-phenyl-3-hexanone (S)-2-bromo-2-methylcyclobutanone 3-methyl-5-(4-chlorophenyl) hexanal 3-isobutylbenzoic acid Acetic butanoic anhydride N-phenyl-N-propyl-2,3-dimethylbutanamide Page 2 o
QUESTION 1 Which of the compounds shown below would be the major organic product of the reaction shown? NH2 Но OH NH2 Он в C D CI CA C c C D ооо
Name the following compounds Acids and Esters homework. 1. Name the following Compounds он OH Brown golon он MacBook A 0. % 5 A 6 7 B 9 0 3 2 P W E R U T Y S D А F G Н. K ? Z с - V N B M Command option option command он OH НО- OH o D MacBook Air A * $ 4 % 5 & 7 3 6 8 9 0 W E...
I need help answering the following questions 1) A compound is insoluble in water, soluble in conc. H2SO4. It shows positive for the 2,4-DNPH test and negative for Chromic Acid test. What do you think the compound is? (3 pts) a) Isopropyl alcohol b) Butyraldehyde c) 3-pentanone d) butan-1-ol 2) Which compound would give a negative result for Iodoform Test? (3 pts) a) t-butyl alcohol b) Acetophenone c) 2-butanol d) Acetaldehyde 3) Which of the following routes can be used...